FDA Inspection 1244904 — Grifols Canada Plasma II Inc.

Grifols Canada Plasma II Inc. — FEI 3002806622

The FDA completed an inspection of Grifols Canada Plasma II Inc. on Jul 16, 2024 in Winnipeg. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 16, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Winnipeg (Canada)